Aliskiren Combined with Losartan in Type 2 Diabetes and Nephropathy
Hans-Henrik Parving, M.D., D.M.Sc., Frederik Persson, M.D., Julia B. Lewis, M.D., Edmund J. Lewis, M.D., Norman K. Hollenberg, M.D., Ph.D., for the AVOID Study Investigators
Background Diabetic nephropathy is the leading cause of end-stagerenal disease in developed countries. We evaluated the renoprotectiveeffects of dual blockade of the renin–angiotensin–aldosteronesystem by adding treatment with aliskiren, an oral direct renininhibitor, to treatment with the maximal recommended dose oflosartan (100 mg daily) and optimal antihypertensive therapyin patients who had hypertension and type 2 diabetes with nephropathy.
Methods We enrolled 599 patients in this multinational, randomized,double-blind study. After a 3-month, open-label, run-in periodduring which patients received 100 mg of losartan daily, patientswere randomly assigned to receive 6 months of treatment withaliskiren (150 mg daily for 3 months, followed by an increasein dosage to 300 mg daily for another 3 months) or placebo,in addition to losartan. The primary outcome was a reductionin the ratio of albumin to creatinine, as measured in an early-morningurine sample, at 6 months.
Results The baseline characteristics of the two groups weresimilar. Treatment with 300 mg of aliskiren daily, as comparedwith placebo, reduced the mean urinary albumin-to-creatinineratio by 20% (95% confidence interval, 9 to 30; P<0.001),with a reduction of 50% or more in 24.7% of the patients whoreceived aliskiren as compared with 12.5% of those who receivedplacebo (P<0.001). A small difference in blood pressure wasseen between the treatment groups by the end of the study period(systolic, 2 mm Hg lower [P=0.07] and diastolic, 1 mm Hg lower[P=0.08] in the aliskiren group). The total numbers of adverseand serious adverse events were similar in the groups.
Conclusions Aliskiren may have renoprotective effects that areindependent of its blood-pressure–lowering effect in patientswith hypertension, type 2 diabetes, and nephropathy who arereceiving the recommended renoprotective treatment. (ClinicalTrials.govnumber, NCT00097955
[ClinicalTrials.gov]
.)
Source Information
From the Department of Medical Endocrinology, Rigshospitalet, Copenhagen (H.-H.P.); the Faculty of Health Science, Aarhus University, Aarhus, Denmark (H.-H.P.); Steno Diabetes Center, Gentofte, Denmark (F.P.); Vanderbilt University School of Medicine, Nashville (J.B.L.); Rush University Medical Center, Chicago (E.J.L.); and Brigham and Women's Hospital and Harvard Medical School, Boston (N.K.H.).
Address reprint requests to Dr. Parving at the Department of Medical Endocrinology, Rigshospitalet, University Hospital of Copenhagen, Blegdamsvej 9, DK-2100 Copenhagen Ø, Denmark, or at hhparving{at}dadlnet.dk.
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